{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Deerfield",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94792",
      "recalling_firm": "Zoll Medical Corporation",
      "address_1": "500 Burdick Pkwy",
      "address_2": "N/A",
      "postal_code": "53531-9692",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide including PR. Foreign: AU BM CA CH DE DK ES FR GB HK HU ID IE IL IT KR MA MT NL NO PR SA SE SI SN TR",
      "recall_number": "Z-2324-2024",
      "product_description": "ZOLL Powerheart G5 AED, Semi-Automatic, G5Sxxx Family -Automated external defibrillator (AED) is designed for treating life-threatening heart beat irregularities, such as ventricular fibrillation, that cause Sudden Cardiac Arrest (SCA).     Model/Catalog Number:    G5S-00A  G5S-00A-TSO  G5S-00C  G5S-01A  G5S-02A  G5S-02C  G5S-02-L  G5S-04A  G5S-05A  G5S-05C  G5S-06A  G5S-06C  G5S-08A  G5S-08C  G5S-10A  G5S-10C  G5S-11A  G5S-11C  G5S-12C  G5S-13A  G5S-14A  G5S-15A  G5S-17A  G5S-17C  G5S-19A  G5S-23C  G5S-29A  G5S-29C  G5S-31A  G5S-31A-SJA  G5S-31C-SJA  G5S-36A  G5S-37A  G5S-41A  G5S-41C  G5S-80A  G5S-80A-TSO  G5S-80C  G5S-80-L  G5S-82A  G5S-82C  G5S-83C  G5S-90C",
      "product_quantity": "14885",
      "reason_for_recall": "G5 Semi-Automatic AED is shipped, with a protective film over its front panel, to protect the screen and  shock button from cosmetic damage during shipping. It has come to our attention that customers may not be removing the protective film during deployment of the product. If the protective film is left adhered to the front bezel it may prevent the user from actuating the shock button and may lead to a delay or prevent delivery of defibrillation therapy to a victim suffering from sudden cardiac arrest",
      "recall_initiation_date": "20240531",
      "center_classification_date": "20240710",
      "report_date": "20240717",
      "code_info": "GTIN: 00812394021239 00812394021277 00812394021284 00812394021413 00812394022779 00847946038182 00847946038199 00847946038243 00847946038250 00847946038304 00847946038328 00847946038335 00847946038342 00847946038359 00847946038380 00847946038397 00847946038403 00847946038410 00847946038434 00847946038441 00847946038496 00847946038519 00847946038533 00847946038571 00847946038588 00847946038663 00847946038816 00847946038830 00847946039028 00847946039035 00847946039066 00847946039127     Serial Number Range: D00000276194-D00000343449"
    }
  ]
}